Ma Ying Long Musk Hemorrhoids Ointment

Manufacturer
Mayinglong Pharmaceutical Group Co., Ltd.
Effective date
2026-07-20
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
daily-update
Hydrated at
2026-09-01 13:03:20

Label at a glance#

ProductMa Ying Long Musk Hemorrhoids
Active ingredientPETROLATUM, ZINC OXIDE
Label structure9 sections

Indications and uses

For the temporary relief of local itching and discomfort associated with hemorrhoids Temporarrily forms a protective coating over inflamed tissue to help prevent drying of tissues. Temporarily protects irritated areas. Temporaily relieves burning. Provides temporary relief from skin irritation. Temporarily provides a coating for relief of anorectal discomforts. Temporarily protects the inflamed, irritated anorecta...

Dosage and administration

Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of the ointment. Apply to the affected area up to 2 times daily or after each bowel movement. Apply liberally to the affected area. FOR INTRARECTAL USE: Attach applicator to tube. Lubricant applicator well with ointment, then g...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Petrolatum 77.99%
Calamine 7.6%

Purpose

OTC - PURPOSE SECTION

Protectant

Astringent

Uses

INDICATIONS & USAGE SECTION

  • For the temporary relief of local itching and discomfort associated with hemorrhoids
  • Temporarrily forms a protective coating over inflamed tissue to help prevent drying of tissues.
  • Temporarily protects irritated areas.
  • Temporaily relieves burning.
  • Provides temporary relief from skin irritation.
  • Temporarily provides a coating for relief of anorectal discomforts.
  • Temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful
  • Temporarily protects inflamed perianal skin.
  • Temporarily relieves the symptoms of perianal skin irritation.

Warnings

WARNINGS SECTION

For external and/or intrarectal use only

Do not use

OTC - DO NOT USE SECTION

  • If allergic to any of the ingredients

When using this product

OTC - WHEN USING SECTION

  • Do not exceed the recommended number of daily uses unless directed by a doctor.
  • Do not use the product with an applicator if the introduction of the applicator into the rectum causes additional pain. Consult a doctor promptly.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Bleeding occurs
  • Condition worsens or does not improve within 7 days

Do not use during pregnancy or when breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

Consult a health professional before use.

Keep out of reach of children to avoid accidental poisoning.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Do not use otherwise than as directed.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of the ointment.
  • Apply to the affected area up to 2 times daily or after each bowel movement.
  • Apply liberally to the affected area.
  • FOR INTRARECTAL USE: Attach applicator to tube. Lubricant applicator well with ointment, then gently insert applicator into the rectum
  • Children under 12 years of age: consult a doctor.

Other information

SPL UNCLASSIFIED SECTION

  • Store at room temperature, 10°C–30°C (50°F - 86°F)
  • Keep the container closed tightly

Inactive ingredients

INACTIVE INGREDIENT SECTION

Amber, Artificial bezoar (Bos Taurus Bile, Cholic Acid, Deoxycholic Acid, Taurine, Bilirubin, Cholesterol), Artificial musk (Muscone), Borax, Borneol, Dimethyl sulfoxide, Lanolin, Pearl

Questions?

OTC - QUESTIONS SECTION

+1-888-296-9067

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

22

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label00Label00

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130040232381232GTIN-13: 0040232381232
EAN-13: 0040232381232
GTIN-12: 040232381232
UPC-A: 040232381232
GTIN storage (14 digits): 00040232381232
Box.jpg
BarcodeEAN-130850058161082GTIN-13: 0850058161082
EAN-13: 0850058161082
GTIN-12: 850058161082
UPC-A: 850058161082
GTIN storage (14 digits): 00850058161082
Label00.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68511-99768511-997-01, 68511-997-02, 68511-997-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
92026-05-13weekly-update2026-07-17 21:43:55
72024-04-22full-release2026-06-01 00:11:21

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ma Ying Long Musk HemorrhoidsPETROLATUM, ZINC OXIDEMayinglong Pharmaceutical Group Co., Ltd.af466f21-c4bc-3b89-e053-2995a90a49f22026-07-20WarningsExact identifier
ndc (package): 68511-997-01
ndc (package): 68511-997-20
ndc (package): 68511-997-02
ndc (product): 68511-997
ndc11 (package): 68511099720
ndc11 (package): 68511099701
ndc11 (package): 68511099702
spl id: 570bace7-35e4-69bd-e063-6394a90a3f7d
spl set id: af466f21-c4bc-3b89-e053-2995a90a49f2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.